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Bioanalysis|July 31, 2015
Integration of bioanalytical measurements using PK-PD modeling and simulation: implications for antibody-drug conjugate developmentAntari Khot, Sharad Sharma, Dhaval K ShahBioanalysis|August 14, 2015
Scientific or regulated validation: a tiered approach? Meeting report from a joint EBF/DVDMDG workshopPhilip Timmerman, Steve Lowes, Stuart McDougall, et al.Bioanalysis|August 14, 2015
The relation of the number of hydrogen-bond acceptors with recoveries of immunosuppressants in DBS analysisRemco A Koster, Jan-Willem C Alffenaar, Rixt Botma, et al.Bioanalysis|August 14, 2015
Linearity of chromatographic systems in drug analysis part II: a Monte Carlo justification for the use of nonlinear regressionsJohn Burrows, Kenneth WatsonBioanalysis|August 14, 2015
Determination of lipoic acid in biological samplesKamila Borowczyk, Marta Krawczyk, Paweł Kubalczyk, et al.Bioanalysis|August 22, 2015
Simultaneous determination of hyzetimibe and its main active metabolite in plasma by LC-MS/MS and its application in PK studyJinliang Chen, Honggang Lou, Bo Jiang, et al.Bioanalysis|March 12, 2016
Oral fluid drug analysis in the age of new psychoactive substancesElisabeth Leere Øiestad, Åse Marit Leere Øiestad, Astrid Gjelstad, et al.Bioanalysis|March 12, 2016
Analytical detection and characterization of biopharmaceutical glycosylation by MSMyung Jin Oh, Serenus Hua, Unyong Kim, et al.Bioanalysis|July 19, 2013
Ask the experts: increasing and maintaining productivity in the bioanalytical laboratoryBrian D Beato, Chad Briscoe, Joe Rajarao, et al.Bioanalysis|May 23, 2012
SPE-MS analysis of absorption, distribution, metabolism and excretion assays: a tool to increase throughput and steamline workflowVaughn P MillerPageof 278